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Comparison of Different Bending Mode for Double-lumen Endotracheal Tube Intubation

Comparison of Different Bending Mode for Double-lumen Endotracheal Tube Intubation

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01605591
Enrollment
66
Registered
2012-05-25
Start date
2011-08-31
Completion date
2012-08-31
Last updated
2014-09-08

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Anesthesia Intubation Complications

Keywords

left-side double lumen bronchial tube, bending type, GlideScope videolaryngoscope

Brief summary

The purpose of this study is to comparing the effects of different double-lumen endotracheal tube's bending type in tracheal intubation.

Detailed description

Intubation with the double-lumen endotracheal tube (DLT) remains a great challenge for anesthesiologists. Although new upper airway devices, such as GlideScope(R) videolaryngoscope, had been developed for facilitating airway management, the larger size and the complexity of DLT than single-lumen tube (SLT) makes the difficulties for DLT intubation. Therefore, the investigators designed this study to investigate the effects of different bending type of DLT in tracheal intubation.

Interventions

PROCEDUREthe DLT bending to the right

bending the bronchial lumen of DLT 60\ 90 degrees in the same side with the tracheal lumen

PROCEDUREthe DLT bending to the left

bending the bronchial lumen of DLT 60\ 90 degree opposed to the tracheal lumen

Sponsors

Kaohsiung Medical University Chung-Ho Memorial Hospital
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
DOUBLE (Investigator, Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
Yes

Inclusion criteria

1. American Society of Anesthesiologists physical status I-III 2. more than 18 years of age 3. Receiving thoracic surgery with double-lumen endobronchial tube

Exclusion criteria

1. risk of regurgitation and pulmonary aspiration 2. history of gastroesophageal reflux 3. pregnancy 4. scheduled tracheostomy and postoperative prolonged ventilation in ICU 5. limited neck extension (\< 35°) 6. a thyromental distance less than 7 cm 7. a sternomental distance less than 12.5 cm with the head fully extended 8. mouth can not open

Design outcomes

Primary

MeasureTime frame
Main outcome measure is the successful rate of the first intubation compared with the two bending modes of DLT12 month

Secondary

MeasureTime frameDescription
mean blood pressure (MAP) before intubation, and after intubation 1, 3,and 5 min12 months
the incidence of hypoxemia during the period of intubation12 monthsHypoxemia is defined as the SPO2 is below 90%.
the time needed to insert the DLT during the period of intubation12 months
the incidence of sore throat after extubation12 months
the incidence of hoarseness after extubation12 months
the heart rate (HR) before intubation, and after intubation 1, 3,and 5 min12 months

Countries

Taiwan

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Mar 7, 2026